Study: Supportive care can improve quality of life for people with metastatic breast cancer
Contents
At a glance | Questions for your doctor |
Findings | In-depth |
Clinical trials | Limitations |
Guidelines | Resources |
STUDY AT A GLANCE
This study is about:
whether a program that provides supportive care to breast cancer patients improves their quality of life and health care experience.
Why is this study important?
breast cancer patients are known to have unique care, treatment, symptom management, and emotional support needs. is an area of medicine focused on improving or preserving quality of life for people facing life-threatening illnesses such as cancer. specialists address a broad range of issues that can affect quality of life and wellbeing. These include pain and symptom management, emotional distress, and advanced care planning, to name a few. This is the first study to evaluate a supportive care program for breast cancer patients.
Study findings:
The Breast Cancer - Support Education and Advocacy (MBC-SEA) program was developed to connect breast cancer patients with existing supportive and educational services.
Data on 118 women with breast cancer were measured before and after the MBC-SEA program was started:
- Patients reported improvements in the following outcomes:
- Fewer or lessened symptoms.
- Decreased anxiety and distress
- Greater overall sense of well-being
- More referrals for social work and (indicating patients were connected with needed services)
- Clinical trial referrals did not increase.
These results were statistically significant. The researchers concluded that support programs like the MBC-SEA can improve care and quality of life for breast cancer patients.
What does this mean for me?
There is growing effort to meet the supportive care needs of cancer patients. If you are experiencing symptoms, side effects, emotional distress or other quality of life issues, ask your doctor for a referral to specialists.
Posted 8/21/19
Share your thoughts on this XRAYS article by taking our brief survey.
References
Reiser V, Rosenzweig M, Welsh A, et al., "The Support, Education and Advocacy (SEA) program of care for women with breast cancer: a nurse-led demonstration program." American Journal of Hospice and Medicine. April 11, 2019. doi: 10.1177/1049909119839696.
Disclosure
FORCE receives funding from industry sponsors, including companies that manufacture cancer drugs, tests and devices. All XRAYS articles are written independently of any sponsor and are reviewed by members of our Scientific Advisory Board prior to publication to assure scientific integrity.
This article is relevant for:
People diagnosed with metastatic breast cancer
This article is also relevant for:
men with breast cancer
people with triple negative breast cancer
people with ER/PR + cancer
people with Her2-positive cancer
Lynch syndrome mutation carrier
people with a genetic mutation linked to cancer risk
people with breast cancer
people with metastatic or advanced cancer
Be part of XRAY:
IN-DEPTH REVIEW OF RESEARCH
Study background:
breast cancer accounts for 6% of all breast cancer cases at diagnosis. Additionally, approximately 30% of women diagnosed at earlier stages will have breast cancer progress to or IV disease.
Women with breast cancer have unique needs compared to those with earlier stages of breast cancer. There are different treatments considerations, palliative concerns as well as distinct psychological, social, financial, and family issues. Primary care or nursing providers often lack time or overview needed to support all aspect of patient needs. There is a growing role for patient nurse navigators (PNN) who may be oncology nurses or social workers or community members who are versed in their field. Prior work has shown that PNNs have been beneficial in coordinating care for patients with other types of cancer or early stages of cancer. The usefulness of PNNs for patients with breast cancer has not been previously tested.
Researchers of this study wanted to know:
whether a program for supportive care for breast cancer patients improves the health care experience.
Populations looked at in this study:
Participants were patients at a Western Pennsylvania cancer care facility. Chart reviews were done for all women who came through the clinic between August and October 2016, 3 months prior to start of the Breast Cancer - Support Education and Advocacy (MBC-SEA) program (186 women), and again 3 months after the program began February to April 2017 (196 women). Women whose charts were reviewed both before and after the MBC-SEA program began were included in the study (118 women). On average, the women in the study were 50-69 years of age, had MBC for 3 years, were receiving hormonal or targeted treatment, and were receptor-positive.
Study design:
The MBC-SEA program was developed to connect breast cancer patients with existing supportive and educational services. A patient nurse navigator (PNN) performed weekly chart reviews for each patient to evaluate treatment status, symptoms, distress, social and financial needs, clinical trial eligibility and counseling needs. The PNN then coordinated supportive services with a collaborative group including practice nurses, nurses, social workers and the clinic team coordinated scheduling and sent clinical reminders for follow up. This allowed targeted, individualize care plans to be developed for each patient.
Data on 118 women with breast cancer were evaluated before and after the MBC-SEA program was started.
Study findings:
Patient reported statistically significant improvements in outcomes using the following:
- The Magee Women's cancer service (MWCS PROcis) symptom inventory evaluates patient-reported outcomes including fatigue, nausea, sleep distress, shortness of breath, dry mouth, sadness, vomiting, numbness or weakness in limbs on a scale of 1 to 10 for each symptom.
- Participants reported fewer or lessened symptoms on the Magee Women's cancer service questionnaire. Scores decreased on average 1.35 (on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- Participants reported fewer or lessened symptoms on the Magee Women's cancer service questionnaire. Scores decreased on average 1.35 (on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- The Generalized Anxiety Disorder (GAD) evaluation measures feelings of nervousness, anxiety, worry, restlessness, irritability and fear.
- Participants reported decreased anxiety and distress on a Generalized Anxiety Disorder evaluation with scores decreasing on average 1.56 ( on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- Participants reported decreased anxiety and distress on a Generalized Anxiety Disorder evaluation with scores decreasing on average 1.56 ( on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- A visual analog scale was used to determine participants overall sense of well-being.
- Participants reported greater overall sense of well-being after the MBC-SEA intervention. Increasing on average 0.7 ( on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- Participants reported greater overall sense of well-being after the MBC-SEA intervention. Increasing on average 0.7 ( on a 10-point scale) after the MBC-SEA intervention compared to before the intervention.
- There were more referrals for social work and (indicating patients were connected with needed services).
- Prior to the MBC-SEA program there were 13 referrals for social work and 14 referrals for . After the MBC-SEA program began, there were 44 referrals for social work and 31 referrals for .
- Prior to the MBC-SEA program there were 13 referrals for social work and 14 referrals for . After the MBC-SEA program began, there were 44 referrals for social work and 31 referrals for .
Clinical trial referrals did not increase.
Limitations:
This study has a number of limitations:
- A major limitation is the size of the study. The intervention included only 118 women with breast cancer. This is a relatively small sample size. This sample size was large enough for the researchers to show statistically significant differences in symptoms, anxiety, overall well-being and referral rates. However, the number of patients is too small to say anything about age, hormone-receptor status, treatment type or other clinical differences. The participants in this study were mostly 50-69 years old, ER+, in hormonal or targeted treatment and from one clinic. Larger studies would be needed to see if these interventions are useful across a broader demographic of patients.
- Another major limitation of this study is that there is no true control group. Responses of patients after the beginning of the MBC-SEA program were compared to their own responses before the MBC-SEA program began. There were no patients that received the prior standard of care during the same time. Because this program is in place and ongoing, it is not possible to reevaluate this program intervention in this location. However, similar programs could be tested in other places.
- This study was conducted at a single cancer clinic in Western Pennsylvania. It is unclear if this intervention program would be similarly effective in other geographic regions given differences in the population of and underlying support services available in different places.
- The patients that were evaluated in this study were patients that were seen in both of two specific 3-month windows. These patients may not be representative of MBC patients as a whole.
- The study researchers point out that the study is limited in that the clinic did not have a standardized threshold for some of the evaluated measure (e.g. distress) that would trigger the referral process. Because of this, there may be some variability in when patients were referred for psychosocial consultations. However, standardized thresholds would be expected to improve differences before and after the intervention.
Conclusions:
The researchers conclude that support intervention programs like the MBC-SEA can improve care and quality of life for breast cancer patients. Additional data on a larger group of patients in other regions would be useful to determine how generalizable these results are.
Share your thoughts on this XRAYS article by taking our brief survey.
Posted 8/21/19
The National Comprehensive Cancer Network (NCCN) Practice Guidelines on Standards of include:
- All cancer patients should be screened for needs at their initial visit, at appropriate intervals and as clinically indicated.
- Patients/families/caregivers should be informed that is an integral part of their comprehensive cancer care.
- specialists should be readily available to provide consultation or direct care to patients/families/caregivers and/or healthcare professionals who request or require their expertise.
Patients, families or caregivers with any of the following conditions or situations should be referred for palliative care:
- uncontrolled symptoms or pain
- moderate-to-severe distress related to diagnosis or treatment
- additional serious physical, psychiatric or psychosocial conditions
- unresolved concerns or lack of understanding about the course of their disease
- advanced cancers
- evidence of worsening prognosis
- communication barriers
- financial limitations
- family discord
Updated: 06/26/2024
- How do I find a specialist?
- I’m experiencing the following (e.g. pain, loss of appetite, anxiety, etc.), can a specialist help me? Does your practice have supportive services available?
- My family member or caregiver is having a difficult time coping with my diagnosis. Can a expert help them?
- What supportive services would you recommend for me?
The following studies are looking at for people diagnosed with cancer:
- Coaching for Family Caregivers of People with Advanced Cancer from Rural and Minority Communities. This study provides coaching to urban African Americans and white or African American families with cancer who live in the rural Southeast. Navigators working with a team provide six health coaching sessions either in person or over the phone to help with managing stress and coping, getting and asking for help, improving caregiving skills and decision-making/advance care planning.
- NCT04733469: EMPOWER 3: Improving Health Literacy and Utilization (EMPOWER 3). This study is designed to test an educational intervention to help patients understand , use it and feel better emotionally and physically.
- NCT04773639: of a Multi-Modal Intervention. This study evaluates a new approach to to address advanced care planning and psychosocial needs of patients with cancer.
- NCT06307535: Study of Meaning-Centered Psychotherapy for Caregivers to People With Cancer. Participants will complete questionnaires and will be assigned to receive psychotherapy for 7 sessions.
- NCT05477784: Cancer Parenting Program for the Enhancement of the Quality of Life of Patients With Advanced Cancer and Their Children (EC-PC). This trial examines the usefulness of two educational programs for parents with cancer who have a 5- to 17-year-old child.
Updated: 06/26/2024